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Clinical Trials/NCT05368272
NCT05368272CompletedNot Applicable

EEG Spectrogram to Assess Brain Vulnerability as a Risk Factor for Postoperative Delirium in Older People - a Feasibility Study

University of Nottingham1 site in 1 country30 target enrollmentStarted: January 27, 2023Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
30
Locations
1
Primary Endpoint
Feasibility of acquiring frontal and posterior EEG data from the Narcotrend monitor during the preoperative and intraoperative period

Study Overview

Brief Summary

An assessment of difference in prespecified processed electroencephalography variables between cognitively intact older surgical patients who develop postoperative delirium compared to those who do not develop postoperative delirium

Detailed Description

Postoperative delirium in older people may be contributed to by intrinsic brain vulnerability such as pre-existing dementia. Some cognitively intact older people also experience postoperative delirium and in these patients some go on to develop later dementia. The investigators propose that postoperative delirium may be an unmasking of covert brain vulnerability by the dyshomeostasis of the anaesthesia/surgical intervention.

In people with dementia or mild cognitive impairment, electroencephalography (EEG) studies have shown slowing of brain wave activity, especially in the back of the brain.

Processed electroencephalography, using a limited number of channels, is routinely used during anaesthesia to aid assessment of anaesthetic depth of the patient.

In this study the investigators will assess the feasibility of acquiring EEG data from the front and back of the brain. The investigators will also explore the data for early signals of brain vulnerability

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • ≥ 65 years old
  • Elective, moderate/major, non-neuro, non-cardiac surgery
  • Ability to give informed consent

Exclusion Criteria

  • Preoperative cognitive impairment
  • Current systemic infection
  • Current use of medication that may modify EEG
  • History of neurosurgery/significant head trauma
  • Presence of neurological diseases including overt stroke, dementia, epilepsy, multiple sclerosis, Parkinson's disease, intracranial tumours and other significant neurologic disorders
  • Current significant psychiatric conditions such as severe depression.
  • Palliative surgery

Outcomes

Primary Outcomes

Feasibility of acquiring frontal and posterior EEG data from the Narcotrend monitor during the preoperative and intraoperative period

Time Frame: Approximately 1 - 2 hours per participant

Feasibility will be assessed by the ability to get preoperative and intraoperative epochs of EEG that clearly demonstrates the different brain wave bands (alpha, theta and delta)

Secondary Outcomes

  • Preoperative brain wave differences(Approximately 10 minutes per participant)
  • Change in brain wave power due to induction of anaesthesia(Approximately 1 hour per particpant)
  • Intraoperative brain wave patterns(Duration of surgery or 2 hours (shortest option))

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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